Canonical Allele Identifier: CA348391712
Gene: ERCC3 HGNC NCBI

Linked Data

dbSNP Id: rs1805161

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127292731T>A , CM000664.2:g.127292731T>A GRCh38
NC_000002.11:g.128050307T>A , CM000664.1:g.128050307T>A GRCh37
NC_000002.10:g.127766777T>A NCBI36
NG_007454.1:g.6446A>T , LRG_462:g.6446A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000285398.7:c.350A>T MANE Select ENSP00000285398.2:p.Lys117Ile
ENST00000642308.1:c.350A>T ENSP00000496684.1:p.Lys117Ile
ENST00000644317.1:c.235-27A>T ENSP00000494012.1:n.235-27A>T
ENST00000645233.1:c.350A>T ENSP00000494116.1:p.Lys117Ile
ENST00000645467.1:c.350A>T ENSP00000494889.1:p.Lys117Ile
ENST00000645736.1:c.206A>T ENSP00000494545.1:p.Lys69Ile
ENST00000646654.1:c.350A>T ENSP00000494526.1:p.Lys117Ile
ENST00000647169.1:c.350A>T ENSP00000495619.1:p.Lys117Ile
ENST00000285398.6:c.350A>T ENSP00000285398.2:p.Lys117Ile
ENST00000426778.5:c.*331A>T ENSP00000415335.1:n.*331A>T
ENST00000445889.5:c.*393A>T ENSP00000390888.1:n.*393A>T
ENST00000462306.5:n.291-27A>T
ENST00000490062.1:n.307-27A>T
ENST00000494464.5:n.261-27A>T
NM_000122.1:c.350A>T , LRG_462t1:c.350A>T NP_000113.1:p.Lys117Ile
NM_001303416.1:c.158A>T NP_001290345.1:p.Lys53Ile
NM_001303418.1:c.158A>T NP_001290347.1:p.Lys53Ile
XM_011510794.1:c.350A>T XP_011509096.1:p.Lys117Ile
XM_011510795.1:c.-80-27A>T XP_011509097.1:n.-80-27A>T
XM_011510794.2:c.350A>T XP_011509096.1:p.Lys117Ile
XM_017003583.1:c.-80-27A>T XP_016859072.1:n.-80-27A>T
NM_000122.2:c.350A>T MANE Select NP_000113.1:p.Lys117Ile
NM_001303416.2:c.158A>T NP_001290345.1:p.Lys53Ile
NM_001303418.2:c.158A>T NP_001290347.1:p.Lys53Ile